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Modafinil

NDC 68788-8280, Modafinil, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8280
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078963
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8280 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MODAFINIL200 mg/1

Pharmacologic classes

Central Nervous System Stimulation [PE]; Increased Sympathetic Activity [PE]; Sympathomimetic-like Agent [EPC]

Package NDCNDC-11Package
68788-8280-36878882800330 TABLET in 1 BOTTLE, PLASTIC (68788-8280-3)
68788-8280-66878882800660 TABLET in 1 BOTTLE, PLASTIC (68788-8280-6)
68788-8280-96878882800990 TABLET in 1 BOTTLE, PLASTIC (68788-8280-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/013450dd-cd42-46c7-98d6-9a2925761978

Use it

Look up 68788-8280 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8280 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8280. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.